GB1297142A - - Google Patents
Info
- Publication number
- GB1297142A GB1297142A GB1297142DA GB1297142A GB 1297142 A GB1297142 A GB 1297142A GB 1297142D A GB1297142D A GB 1297142DA GB 1297142 A GB1297142 A GB 1297142A
- Authority
- GB
- United Kingdom
- Prior art keywords
- triisobutyltin
- trioctyltin
- octyl
- hydroxide
- compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000002253 acid Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- RJWMXZPGQZMQEV-UHFFFAOYSA-M tris(2-methylpropyl)stannanylium;hydroxide Chemical compound [OH-].CC(C)C[Sn+](CC(C)C)CC(C)C RJWMXZPGQZMQEV-UHFFFAOYSA-M 0.000 abstract 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- XATCWUIVPWOLDP-UHFFFAOYSA-N trioctyl(trioctylstannyloxy)stannane Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)O[Sn](CCCCCCCC)(CCCCCCCC)CCCCCCCC XATCWUIVPWOLDP-UHFFFAOYSA-N 0.000 abstract 2
- JNVFIMNBBVDEPV-UHFFFAOYSA-N 4-butylbenzenesulfonic acid Chemical compound CCCCC1=CC=C(S(O)(=O)=O)C=C1 JNVFIMNBBVDEPV-UHFFFAOYSA-N 0.000 abstract 1
- QLYDLSJHTFXHPZ-UHFFFAOYSA-M C(CCC)C1=CC=C(C=C1)S(=O)(=O)[O-].C(C(C)C)[Sn+](CC(C)C)CC(C)C Chemical compound C(CCC)C1=CC=C(C=C1)S(=O)(=O)[O-].C(C(C)C)[Sn+](CC(C)C)CC(C)C QLYDLSJHTFXHPZ-UHFFFAOYSA-M 0.000 abstract 1
- MWOFIYUMYCFIEZ-UHFFFAOYSA-L CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC.CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC.CN.[O-]C(CCC([O-])=O)=O Chemical compound CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC.CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC.CN.[O-]C(CCC([O-])=O)=O MWOFIYUMYCFIEZ-UHFFFAOYSA-L 0.000 abstract 1
- 101100366000 Caenorhabditis elegans snr-1 gene Proteins 0.000 abstract 1
- IJFPVINAQGWBRJ-UHFFFAOYSA-N Diisooctyl phthalate Chemical compound CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C IJFPVINAQGWBRJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- XWIPPCILKVDJHV-UHFFFAOYSA-N azane;naphthalene-1,5-disulfonic acid Chemical compound [NH4+].[NH4+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1S([O-])(=O)=O XWIPPCILKVDJHV-UHFFFAOYSA-N 0.000 abstract 1
- SNAMIIGIIUQQSP-UHFFFAOYSA-N bis(6-methylheptyl) hydrogen phosphate Chemical group CC(C)CCCCCOP(O)(=O)OCCCCCC(C)C SNAMIIGIIUQQSP-UHFFFAOYSA-N 0.000 abstract 1
- AQJOZAJPXQJEBJ-UHFFFAOYSA-M bis(6-methylheptyl) phosphate tris(2-methylpropyl)stannanylium Chemical compound P(=O)(OCCCCCC(C)C)(OCCCCCC(C)C)[O-].C(C(C)C)[Sn+](CC(C)C)CC(C)C AQJOZAJPXQJEBJ-UHFFFAOYSA-M 0.000 abstract 1
- LYGHEAFUHNXUGV-UHFFFAOYSA-N butanedioate;methylazanium Chemical compound [NH3+]C.[NH3+]C.[O-]C(=O)CCC([O-])=O LYGHEAFUHNXUGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 abstract 1
- VUQUOGPMUUJORT-UHFFFAOYSA-N methyl 4-methylbenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C(C)C=C1 VUQUOGPMUUJORT-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003606 tin compounds Chemical class 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 abstract 1
- HJNBKKMVQZKRNU-UHFFFAOYSA-M trioctylstannyl acetate Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)OC(C)=O HJNBKKMVQZKRNU-UHFFFAOYSA-M 0.000 abstract 1
- UGEBTGZCEBOXJS-UHFFFAOYSA-N trioctyltin Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)[Sn](CCCCCCCC)(CCCCCCCC)CCCCCCCC UGEBTGZCEBOXJS-UHFFFAOYSA-N 0.000 abstract 1
- XBPQKEVXCHKRSW-UHFFFAOYSA-N tris(2-methylpropyl)tin Chemical compound CC(C)C[Sn](CC(C)C)CC(C)C XBPQKEVXCHKRSW-UHFFFAOYSA-N 0.000 abstract 1
- FSLSJTZWDATVTK-UHFFFAOYSA-N tris(6-methylheptyl) phosphate Chemical compound CC(C)CCCCCOP(=O)(OCCCCCC(C)C)OCCCCCC(C)C FSLSJTZWDATVTK-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
1297142 Trialkyl and triaryl tin compounds UNITIKA Ltd and N SAITO 21 Nov 1969 [22 Nov 1968 10 Feb 1969] 57017/69 Heading C2J [Also in Division D1] Organotin compounds for imparting antistatic properties to fabrics (see Division D1) have the formula AOSnR 1 R 1 R 2 where R 1 and R 2 are alkyl, aryl or aralkyl and A is a residue obtained by removal of OH from a mono- or dialkyl phosphate or phosphite, a monocarboxylic or dicarboxylic acid, a dicarboxylic acid monoalkyl ester, a monosulphonic or disulphonic acid, a disulphonic acid monoalkyl ester or an alkylsulphuric acid. The compounds may be prepared by reaction between compounds AOX and YOSnR 1 R 1 R 2 , where X=H, NH 4 , or alkyl and Y=H, SnR 1 R 1 R 2 or alkanoyl, by mixing in an organic solvent at room temperature or somewhat above, optionally in contact with the fabric to be treated. The following preparations are specified in the examples: (1), (2), (5) and (9) triisobutyltin diiso-octyl phosphate from triisobutyltin hydroxide and diiso-octyl or triisooctyl phosphate, (3) and (6) triisobutyltin isooctylphthalate from triisobutyltin hydroxide and monoiso-octyl or diiso-octyl 0-phthalate, (4) and (8) triisobutyltin 4-butylbenzenesulphonate from triisobutyltin hydroxide and 4- butylbenzenesulphonic acid or its methyl ester, (7) p-toluenesulphonate from methyl p-toluenesulphonate and triphenyltin hydroxide, (10)- (13) trioctyltin naphthalene-1,5-disulphonate from diammonium naphthalene-1,5-disulphonate and bis-(trioctyltin) oxide or trioctyltin acetate, (14) bis-(trioctyltin) methylammonium succinate from bis-(trioctyltin) oxide and methylammonium succinate.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8587468 | 1968-11-22 | ||
| JP996769 | 1969-02-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1297142A true GB1297142A (en) | 1972-11-22 |
Family
ID=26344802
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1297142D Expired GB1297142A (en) | 1968-11-22 | 1969-11-21 |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE1958639A1 (en) |
| FR (1) | FR2023917A1 (en) |
| GB (1) | GB1297142A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115078605A (en) * | 2022-06-15 | 2022-09-20 | 宁波中普检测技术服务有限公司 | Method for detecting isooctyl thioglycolate di-n-octyl tin in polyvinyl chloride plastic |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3215413A1 (en) * | 1982-04-24 | 1983-10-27 | Bayer Ag, 5090 Leverkusen | METALIZED POLYMER GRANULES, THEIR PRODUCTION AND USE |
| AR243195A1 (en) * | 1985-09-03 | 1993-07-30 | Shionogi & Co Ltd Y Nitto Kase | Tri-organo-tin compounds and pesticide compounds that contain them. |
-
1969
- 1969-11-21 GB GB1297142D patent/GB1297142A/en not_active Expired
- 1969-11-21 DE DE19691958639 patent/DE1958639A1/en active Pending
- 1969-11-21 FR FR6940187A patent/FR2023917A1/fr not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115078605A (en) * | 2022-06-15 | 2022-09-20 | 宁波中普检测技术服务有限公司 | Method for detecting isooctyl thioglycolate di-n-octyl tin in polyvinyl chloride plastic |
| CN115078605B (en) * | 2022-06-15 | 2024-01-02 | 宁波中普检测技术服务有限公司 | Method for detecting isooctyl thioglycolate di-n-octyl tin in polyvinyl chloride plastic |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1958639A1 (en) | 1970-06-18 |
| FR2023917A1 (en) | 1970-08-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |